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HS Code |
659797 |
| Productname | 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester |
| Casnumber | 857365-57-4 |
| Molecularformula | C11H14BBrFNO2 |
| Molecularweight | 301.95 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Storageconditions | Store at 2-8°C, protected from light and moisture |
| Chemicalsynonyms | Pinacol 5-bromo-2-fluoropyridin-3-ylboronate |
| Smiles | CC1(C)OB(C2=CN=C(C(=C2)Br)F)OC1(C)C |
| Inchikey | NDGFUAKZEYAMSS-UHFFFAOYSA-N |
As an accredited 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 5 g of 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester is supplied in a sealed amber glass vial with a printed label. |
| Container Loading (20′ FCL) | 20′ FCL container holds securely packed drums of 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester for safe, efficient shipping. |
| Shipping | 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester is shipped in sealed containers under inert atmosphere, typically at ambient temperature. The packaging ensures protection from moisture and light. It is classified as a non-hazardous material but should be handled according to standard chemical safety protocols. Shipping complies with all relevant regulatory and labeling requirements. |
| Storage | 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester should be stored in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances. Keep the container tightly closed and protected from light and moisture. Store at room temperature or as specified by the manufacturer, and avoid prolonged exposure to air to maintain its stability and prevent decomposition. |
| Shelf Life | **Shelf Life:** Stable for at least 2 years when stored in a cool, dry place, tightly sealed, and protected from light and moisture. |
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Purity 98%: 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester with 98% purity is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high product yield and selectivity. Melting Point 87-90°C: 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester with a melting point of 87-90°C is used in pharmaceutical intermediate synthesis, where it promotes reliable solid-state handling during scale-up. Particle Size <40 μm: 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester with particle size below 40 μm is used in automated solid-phase synthesis, where it allows for rapid dissolution and homogeneous reaction mixtures. Moisture Content <0.5%: 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester with moisture content under 0.5% is used in air-sensitive organometallic procedures, where it provides reproducible reaction conditions and minimizes hydrolysis. Stability Temperature up to 50°C: 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester stable up to 50°C is used in multi-step synthesis workflows, where it maintains integrity and consistent reactivity during intermediate storage. |
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Every chemical manufacturer knows that small changes in molecular structure can transform a synthetic route. Years in the lab have taught us the importance of starting materials that don’t just meet a spec sheet but actually perform when reactions get complex. Among the boronic esters, 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester stands out for a chemist who demands reliable cross-coupling and functional group compatibility. We produce this compound in-house, closely tracking purity and controlling each variable. It turns up on the bench over and over again in research and pharmaceutical projects needing aromatic ring sophistication—especially in heterocycle development or when optimizing halogenated intermediates.
Work in process chemistry rarely runs on textbook reactions. Problems pop up—steric hindrance, hydrolysis, overheating, and the unpredictability that comes when scaling boronic acid derivatives. That’s the context behind focusing on the pinacol ester of 5-Bromo-2-fluoropyridine-3-boronic acid. Unlike the free acid, the pinacol ester format gives stability in the flask, shipping, and storage, making it far less sensitive to moisture and temperature swings. During Suzuki coupling, that translates into less decomposition and cleaner reactions. For our teams, that consistency means less rework, more robust yields, and fewer repeated purifications.
The bromo and fluoro substituents on the pyridine ring open up design space that other boronates just don’t offer. Pairing the electron-withdrawing effect from fluorine with bromine’s reactivity lets chemists pursue orthogonal cross-couplings and metalations. We have witnessed how medicinal chemistry groups rely on the specificity 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester brings, allowing them to build out SAR libraries or introduce tailored modifications on nitrogen-containing rings.
Anyone familiar with large-scale reactions understands that purity impacts everything from isolated yield to regulatory acceptance. Our production adheres to rigorous checks—NMR, HPLC, and GC evaluations at each stage. Minor impurities or isomer content can destroy a project’s momentum. As a manufacturer, traceability stretches back to the raw material intake, with every lot mapped for impurities that might sneak through. We select solvents and reagents based on thorough prior qualification—not based solely on literature precedent. Decades of hands-on manufacturing have shaped how we control our synthesis environment. Whether the client runs a 100 g prep or a kilo batch, our experience guides every risk management decision—we do not gamble with impurities or cross-contamination.
Organoboron chemistry has exploded for a reason, yet some boronic acids frustrate more than facilitate. Traditional boronic acids hydrolyze in the presence of ambient water, degrade on the shelf, and dish out batch-to-batch variability that limits their shelf life. Pinacol esters, by contrast, stay reliable for months—sometimes years—under proper storage. We have watched clients attempt “off-the-rack” boronic acids from warehouse suppliers, only to lose weeks investigating side reactions or purity issues. Overcoming such challenges compelled us to stick with the pinacol ester derivative, verifying its thermal and hydrolytic stability under actual process conditions, not just in a QC lab.
Other pyridine boronates often leave project teams with lower regioselectivity and less functional handle diversity. Here, the bromine enables straightforward palladium catalysis, coupling with aryl and vinyl halides under typical Suzuki-Miyaura conditions. The fluorine on the pyridine gives additional electronic tuning, which has shown itself beneficial for tuning the physicochemical properties of advanced intermediates, affecting solubility, reactivity, and downstream biological activity. Chemists aiming for multi-step syntheses appreciate having multiple positions on the pyridine activated for future functionalization, instead of being locked into a limited scope.
Scalability separates theory from reality. In our early days scaling pinacol ester production, common issues included inefficient drying, variable filtration rates, pinacol hydrolysis under atmospheric conditions, and occasional exotherms during boronic acid condensation. We resolved these in our facility by refining reaction times and switching to high-efficiency vacuum systems for water removal. The resulting batches showed narrower melting point ranges, and our team documented increased shelf stability. Those changes did not come overnight; they took countless iterations and process tweaks based on firsthand lessons. In turn, that practical knowledge flows back upstream to research teams needing reproducible outcomes.
Many competitors take their cues from literature protocols, assuming small-scale reactions transfer to the plant floor with minor tweaks. Real manufacturing reveals a tougher truth—selecting the right boronic acid source, maintaining strict moisture controls, and overseeing every wash all bank on experience, not guesswork. From our vantage point, each kilogram of 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester we ship carries that commitment to process discipline. It is about making sure our material arrives with properties undiminished, no matter the distance or season.
Every stage in a plant dealing with boronic esters brings its own risks. Unintentional contact with water, oxygen, or elevated temperatures—even for a day—produces side products and breaks down the pinacol ester. To counteract those risks, we implemented desiccant-controlled storage and invested in climate-stable warehousing. Only by tracking each bulk drum and keeping sampling air-tight do we meet both our in-house standards and our clients' expectations.
In larger synthesis campaigns, the choice of solvent and the palladium source makes or breaks process throughput. We’ve found that toluene and isopropanol mixtures work best for loading the ester into reactors. Agitation speed, base choice, and phase separation then follow direct experience instead of theory. The pinacol ester’s solubility profile helps avoid stubborn emulsions, and its compatibility with automated liquid handlers streamlines workflow for clients running parallel synthesis or continuous processes. Over time, our firsthand adaptation at scale became a playbook for clients with similar needs—turnkey solutions engineered from years of trial, error, and observation, not from one-size-fits-all industry templates.
Academic labs and process R&D teams both look for versatile, stable boronic esters in their workflows. We’ve seen this compound anchor the preparation of advanced pharmaceutical intermediates and agrochemical candidates, supporting everything from small-molecule kinase inhibitors to insecticide scaffolds. Its role extends beyond Suzuki coupling; the pyridine core lends itself to metal-catalyzed aminations, direct arylation, and photoredox reactions that expand the scope of transition metal chemistry.
Collaborations with pharmaceutical innovation groups often focus on late-stage functionalization. Time and again, the 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester features in these projects thanks to its blend of stability and selectivity. We’ve helped customers bypass scale-up pitfalls by recommending optimized catalytic cycles and sharing lessons learned from our pilot campaigns. For instance, tweaking ligand loading or introducing extra water scavengers allowed teams to push transformations that would otherwise stall with more finicky boronic acids.
In the past, organic chemists chasing pyridine coupling partners spent most of their effort troubleshooting reaction failures. With a more robust pinacol ester—compared to a free boronic acid or unstable alternatives—fewer reactions fail unpredictably. Several customers told us how this format simplified their logistics and enabled more reliable screening. Researchers run more reactions before degradation becomes a risk, giving them flexibility in planning experiments or running secondary screens on a new target series.
Process engineering teams working with us notice less gassing, foaming, or kettle fouling during scale-up when using this ester format. Its semi-crystalline nature means easier handling and less dusting in charging operations, which pays off in cleaner workspaces and less material loss. All these factors matter to actual users but rarely surface in datasheets. For researchers in a regulated space—thinking ahead to validation and eventual audits—batch records and impurity profiles for the pinacol ester are easier to justify given the format’s resistance to degradation under the most typically encountered stress conditions.
Customers continue to push for shorter synthetic cycles, purer intermediates, and robust regulatory defensibility. We respond through continuous process improvement, never settling for generic supply or chemical “commoditization.” Requests for data don’t just drop into an inbox—we treat every question on handling, shelf life, or scalability as a practical problem. Several pharma partners have collaborated with our technical team to adapt points raised in standard operating procedures, stability studies, and transportation protocols. In those joint reviews, the practical experience always outweighs theoretical case studies. For example, optimizing nitrogen purging on larger reactors cut hydrolytic decomposition by half, streamlining R&D budgets and headcount needs at the customer’s facility. Such results build trust, and—over time—drive long-term supply partnerships based on competence and transparency, not mere catalog pricing or intermediaries.
Regulations keep evolving, and meeting ever-tightening purity specs isn’t optional for any manufacturer. Our in-house quality assurance covers not just product release specs but continuous environmental monitoring and operator training. Sustainable pinacol ester production benefits from optimizing solvent recovery, recycling washes, and reducing waste streams through process intensification. We document and share the results of these sustainability efforts with customers who care about more than headline purity. By investing in cleaner reactant sourcing and closed-loop solvent management, we minimize both manufacturing cost and environmental impact. We see these steps pay off in smoother audits and a more reliable, future-proof supply chain.
One lesson stands out: shortcuts serve no one in specialty chemical manufacturing. Each step—from sourcing starting materials to packaging the final product—demands discipline and knowledge gained from mistakes, not only from instructions. When a batch fails, we analyze every variable. Whether it means revising a synthesis step, recalibrating analytical equipment, or updating an SOP, we treat corrective action as a critical source of expertise.
Every successful lot of 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester goes through human-led QC, hands-on process inspections, and batch-level data review. We keep extensive records, not to satisfy paperwork alone, but to track trends and support failure analysis that drives improvements. By sharing lessons openly with our partners, we help them avoid common pitfalls and focus on the chemistry that truly matters to their development pipeline.
We never lose sight of our end users—a medicinal chemist juggling a stacked reaction queue or a process engineer planning a major scale-up. We know that keeping batches shipping on time, communicating any supply chain ripple, and providing technical backup always outweighs generic assurances. We keep a tight feedback loop with clients, often learning from their downstream experiments and integrating fresh insights back into manufacturing design. That hands-on, craft-based approach—more than shiny brochures or industry soundbites—keeps our product relevant and trusted by people making real compounds in real labs and plants.
Choosing 5-Bromo-2-fluoropyridine-3-boronic acid, pinacol ester means fewer surprises in the plant, smoother scale-up, and cleaner product at every step. Compared to generic pyridine boronic acids or non-pinacol esters, our format handles moisture better, lasts longer on the shelf, and performs more predictably in typical cross-couplings. Regular users in pharma, agrochemical, and academic settings report cutting both rework and waste rates. That’s the sort of feedback that shapes every technical and operational decision we make, not just at the bench, but throughout the factory floor and shipping docks. As manufacturers, our commitment and expertise travel with each shipment, shaped by real chemistry—not industry templates or trading practices.